Allele Registry

Canonical Allele Identifier: PA916057237

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000079207

RCV000254892

RCV000492165

RCV001034687

ClinVar Variation:

93326

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Asn78Ser	CA020131 NM_198156.3:c.233A>G